The effects of replacing L-pyroglutamic acid with the cyclopropane analogue 2,3-methanopyroglutamic acid (2,3-MeGlp) on conformation and enzymatic stability have been investigated in 2,3-MeGlp-NHMe and the novel thyrotropin releasing hormone (TRH) analogue [2,3-MeGlp1]-TRH by x-ray diffraction and n
X-Ray conformational study of hydrazino peptide analogues
✍ Scribed by André Aubry; Daniel Bayeul; Jean-Paul Mangeot; Joëlle Vidal; Sébastien Sterin; André Collet; Alain Lecoq; Michel Marraud
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1991
- Tongue
- English
- Weight
- 490 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
We have solved the crystal structures of nine pseudo-peptide analogues deriving from the hydrazino analogue of glycine or valine (NBH2-N"H-C"HR-C02H, R = H or i P r ) or proline ( NBH2-N"-C"H-C02H) and containing the hydrazide ( CO-NOH-N" <) or N@-Z-aminoamide [ CO-N"( NBHZ)] peptidomimetic link. This study gives access to the average geometry of these two links, to their inter-and intramolecular interaction modes, and to their influence on the conformational properties of the molecules.
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